A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251286



Internal ID20818326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67620305..67620931hg38UCSC Ensembl
chr1:68085988..68086614hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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